Cuprum Quartz (Metallic)
- Product NDC
- 48951-3153
- 11-digit product format
- 489513153
- Labeler code
- 48951
- Product ID
- 48951-3153_da314ac9-4b8c-41fc-a3cb-329de4089be7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cuprum Quartz (Metallic)
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- COPPER
- Active strength
- 1 [hp_X]/g
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 48951-3153-5 | Cuprum Quartz (Metallic) | 60 g in 1 TUBE | OINTMENT | 60 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48951-3153 | CUPRUM QUARTZ (METALLIC) OINTMENT [URIEL PHARMACY INC.] | 1 | Legacy NDC, 1 package rows | 20140904_a957dd20-09b5-45c7-ab4d-718f8789dd48.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 48951-3153-5 | 48951315305 | 60 g in 1 TUBE | 60 g | Historical |